Recent Progress of Substituted Allylboron Compounds in Catalytic Asymmetric Allylation Reactions

被引:0
|
作者
Tang, Xiaoxue [1 ]
Chen, Yushuang [2 ]
Huang, Jingbin [1 ]
机构
[1] Army Med Univ, Dept Pharm, Affiliated Hosp 2, Chongqing 400037, Peoples R China
[2] Chongqing Univ Sci & Technol, Sch Chem & Chem Engn, Chongqing 401331, Peoples R China
来源
CHEMICAL RECORD | 2025年 / 25卷 / 03期
关键词
asymmetric allylation reactions; allylboron reagents; gamma-selectivity; alpha-selectivity; natural products; STEREOSELECTIVE-SYNTHESIS; ENANTIOSELECTIVE ALLYLATION; QUATERNARY STEREOCENTERS; HOMOALLYLIC ALCOHOLS; CARBONYL-COMPOUNDS; CYCLIC IMINES; CONSTRUCTION; DERIVATIVES; PHOSPHATES; MOLECULES;
D O I
10.1002/tcr.202400208
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalytic asymmetric allylation reaction involving allylboron species has emerged as a powerful tool to access highly stereoselective allylation products. In the early years, most of the researches focused on the reaction of unsubstituted allylboronates with ketones or imines. With the synthesis of complex substituted allylboronates, allylboronic acids and allyltrifluoroborates, the type of reactions and the variety of substrates are greatly expanded. Therefore, this review article will emphasize on the aspect of regio- and stereoselectivity when substituted allylboron species involving and their application on the construction of versatile organic building blocks, drugs and natural products.
引用
收藏
页数:16
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